Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation
© 2018, Springer-Verlag GmbH Austria, part of Springer Nature. Abstract: A simple and efficient procedure for the synthesis of substituted imidazo[1,2-a]pyridines under ultrasound irradiation has been developed. The reactions were carried out using ionic liquids as catalyst. The reaction procedure d...
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th-cmuir.6653943832-626272018-11-29T07:36:19Z Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation Piyawat Paengphua Sirirat Chancharunee Chemistry © 2018, Springer-Verlag GmbH Austria, part of Springer Nature. Abstract: A simple and efficient procedure for the synthesis of substituted imidazo[1,2-a]pyridines under ultrasound irradiation has been developed. The reactions were carried out using ionic liquids as catalyst. The reaction procedure demonstrated a broad substrate scope for both acetophenones and 2-aminopyridines, and provided convenient access to a wide variety of imidazo[1,2-a]pyridines. The present method offers several advantages compared to traditional heating methods such as higher yields, shorter reaction times, milder reaction conditions, and easier work-up procedure. Graphical abstract: [Figure not available: see fulltext.]. 2018-11-29T07:36:19Z 2018-11-29T07:36:19Z 2018-10-01 Journal 00269247 2-s2.0-85052616175 10.1007/s00706-018-2238-3 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052616175&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62627 |
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Chemistry Piyawat Paengphua Sirirat Chancharunee Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation |
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© 2018, Springer-Verlag GmbH Austria, part of Springer Nature. Abstract: A simple and efficient procedure for the synthesis of substituted imidazo[1,2-a]pyridines under ultrasound irradiation has been developed. The reactions were carried out using ionic liquids as catalyst. The reaction procedure demonstrated a broad substrate scope for both acetophenones and 2-aminopyridines, and provided convenient access to a wide variety of imidazo[1,2-a]pyridines. The present method offers several advantages compared to traditional heating methods such as higher yields, shorter reaction times, milder reaction conditions, and easier work-up procedure. Graphical abstract: [Figure not available: see fulltext.]. |
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Piyawat Paengphua Sirirat Chancharunee |
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Piyawat Paengphua Sirirat Chancharunee |
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Piyawat Paengphua |
title |
Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation |
title_short |
Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation |
title_full |
Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation |
title_fullStr |
Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation |
title_full_unstemmed |
Facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation |
title_sort |
facile synthesis of imidazo[1,2-a]pyridines promoted by room-temperature ionic liquids under ultrasound irradiation |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052616175&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62627 |
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